Fused polycyclic heteroaromatic compound, organic thin film including compound and electronic device including organic thin film

ABSTRACT

A fused polycyclic heteroaromatic compound is represented by one of Chemical Formula 1, 2A and 2B.

CROSS-REFERENCE TO RELATED APPLICATION

This application is a divisional of U.S. application Ser. No.15/172,875, filed on Jun. 3, 2016, which claims priority to the benefitof Korean Patent Application No. 10-2015-0142418 filed in the KoreanIntellectual Property Office on Oct. 12, 2015, the entire contents ofeach of the above-referenced applications are herein incorporated byreference.

BACKGROUND

1. Field

Example embodiments relate to a fused polycyclic heteroaromaticcompound, an organic thin film including the same, and an electronicdevice including the organic thin film.

2. Description of the Related Art

Flat display devices, e.g., liquid crystal displays or organicelectroluminescent displays, are provided with a variety of thin filmtransistors (TFTs) to drive them. The TFT may include a gate electrode,source/drain electrodes, and a semiconductor layer that may be activatedin response to the operation of the gate electrode. The semiconductorlayer may include an organic semiconductor material that is controlledby a current between the source electrode and the drain electrode usingan applied gate voltage.

Recently, there has been research on a low-molecular-weight organicmaterial, e.g., pentacene, or a polymer organic material, e.g.,polythiophene, as an organic semiconductor material to be used for achannel of a thin film transistor.

However, the polymer organic material has lower charge mobility and ahigher off-state leakage current. On the other hand, thelow-molecular-weight organic material, for example, pentacene isreported to have higher charge mobility of greater than or equal toabout 3.2 to about 5.0 cm²/Vs but needs expensive vacuum depositionequipment to form a thin film, and thus may not be appropriate in termsof processability and formation of a larger area.

Accordingly, development of a new organic semiconductor materialsimultaneously having improved electrical characteristics andprocessability is continuously required.

SUMMARY

Example embodiments provide a relatively low-molecular-weight fusedpolycyclic heteroaromatic compound that has a compact planar structurein which aromatic rings are fused together and that includes nitrogen atan outmost aromatic ring and/or in a center aromatic ring, and therebyexhibits relatively high charge mobility, and furthermore, enables theuse of a deposition process or a room-temperature (about 20° C. to about25° C.) solution process when applied to devices, therefore realizingimproved processability.

Example embodiments also provide an organic thin film including thefused polycyclic heteroaromatic compound.

Example embodiments also provide an electronic device including theorganic thin film as a carrier transport layer.

According to example embodiments, a fused polycyclic heteroaromaticcompound is represented by Chemical Formula 1.

In Chemical Formula 1,

each of X¹ and X² is independently one of S, Se, and Te,

each of Y¹ to Y⁸ is independently one of nitrogen (N) and C—R^(a),wherein R^(a) is one of hydrogen and a linear or branched C₁ to C₁₀alkyl group, provided that at least one of Y¹ to Y⁴ and at least one ofY⁵ to Y⁸ are nitrogen, and

each of R¹ to R⁴ is independently one of hydrogen, a substituted orunsubstituted C₁ to C₃₀ alkyl group, a substituted or unsubstituted C₆to C₃₀ aryl group and a substituted or unsubstituted C₂ to C₃₀heteroaryl group, a substituted or unsubstituted C₇ to C₃₀ arylalkylgroup, a substituted or unsubstituted C₂ to C₃₀ heteroarylalkyl group, asubstituted or unsubstituted C₂ to C₃₀ alkylheteroaryl group, asubstituted or unsubstituted C₅ to C₃₀ cycloalkyl group, and asubstituted or unsubstituted C₂ to C₃₀ heterocycloalkyl group.

In Chemical Formula 1, at least one of Y¹ to Y⁴ may be a first nitrogenand at least one of Y⁵ to Y⁸ may be a second nitrogen, and the firstnitrogen and the second nitrogen may be facing each other.

In Chemical Formula 1, at least two of Y¹ to Y⁴ may be nitrogen and atleast two of Y⁵ to Y⁸ may be nitrogen.

The fused polycyclic heteroaromatic compound may have a molecular weightof about 300 to about 3000.

The fused polycyclic heteroaromatic compound represented by ChemicalFormula 1 may include, for example, at least one of compounds (1) to (8)represented by Chemical Formula 1-1.

In Chemical Formula 1-1,

a hydrogen of each aromatic ring may be replaced by a substituent, forexample a substituted or unsubstituted C₁ to C₃₀ linear or branchedalkyl group, a substituted or unsubstituted C₆ to C₃₀ aryl group and asubstituted or unsubstituted C₂ to C₃₀ heteroaryl group, a substitutedor unsubstituted C₇ to C₃₀ arylalkyl group, a substituted orunsubstituted C₂ to C₃₀ heteroarylalkyl group, a substituted orunsubstituted C₂ to C₃₀ alkylheteroaryl group, a substituted orunsubstituted C₅ to C₃₀ cycloalkyl group, and a substituted orunsubstituted C₂ to C₃₀ heterocycloalkyl group.

According to example embodiments, a fused polycyclic heteroaromaticcompound is represented by one of Chemical Formula 2A and 2B.

In Chemical Formulae 2A and 2B,

each of X³ and X⁴ is independently one of S, Se, and Te,

each of R^(1a) and R^(1b) is independently one of hydrogen and a linearor branched C₁ to C₁₀ alkyl group, and

each of R¹² to R¹⁹ is independently one of hydrogen, a substituted orunsubstituted C₁ to C₃₀ alkyl group, a substituted or unsubstituted C₆to C₃₀ aryl group and a substituted or unsubstituted C₂ to C₃₀heteroaryl group, a substituted or unsubstituted C₇ to C₃₀ arylalkylgroup, a substituted or unsubstituted C₂ to C₃₀ heteroarylalkyl group, asubstituted or unsubstituted C₂ to C₃₀ alkylheteroaryl group, asubstituted or unsubstituted C₅ to C₃₀ cycloalkyl group, and asubstituted or unsubstituted C₂ to C₃₀ heterocycloalkyl group.

The fused polycyclic heteroaromatic compound represented by ChemicalFormula 2A or 2B may include at least one of compounds (9) to (12)represented by Chemical Formula 2-1.

In Chemical Formula 2-1,

hydrogen of each aromatic ring may be replaced by a substituent, forexample one of a substituted or unsubstituted C₁ to C₃₀ linear orbranched alkyl group, a substituted or unsubstituted C₆ to C₃₀ arylgroup and a substituted or unsubstituted C₂ to C₃₀ heteroaryl group, asubstituted or unsubstituted C₇ to C₃₀ arylalkyl group, a substituted orunsubstituted C₂ to C₃₀ heteroarylalkyl group, a substituted orunsubstituted C₂ to C₃₀ alkylheteroaryl group, a substituted orunsubstituted C₅ to C₃₀ cycloalkyl group, and a substituted orunsubstituted C₂ to C₃₀ heterocycloalkyl group.

According to example embodiments, an organic thin film and an electronicdevice include the fused polycyclic heteroaromatic compound.

The electronic device may be one of a transistor, an organic lightemitting diode (OLED), a photovoltaic device, a solar cell, a laserdevice, a memory device, and a sensor.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 is a schematic cross-sectional view showing a transistoraccording to example embodiments.

FIG. 2 is a schematic cross-sectional view showing a transistoraccording to example embodiments.

FIG. 3 shows a MALDI-MS analysis result of the compound (1) synthesizedaccording to Example 1.

FIG. 4 shows a thermogravimetric analysis result (TGA) of the compound(1) synthesized according to Example 1.

DETAILED DESCRIPTION

The present disclosure will be described more fully hereinafter withreference to the accompanying drawings, in which example embodiments areshown. However, this disclosure may be embodied in many different formsand is not construed as limited to the example embodiments set forthherein.

In the drawings, the thickness of layers, films, panels, regions, etc.,are exaggerated for clarity.

It will be understood that when an element such as a layer, film,region, or substrate is referred to as being “on” another element, itmay be directly on the other element or intervening elements may also bepresent. In contrast, when an element is referred to as being “directlyon” another element, there are no intervening elements present.

It should be understood that, although the terms first, second, third,etc. may be used herein to describe various elements, components,regions, layers and/or sections, these elements, components, regions,layers, and/or sections should not be limited by these terms. Theseterms are only used to distinguish one element, component, region,layer, or section from another region, layer, or section. Thus, a firstelement, component, region, layer, or section discussed below could betermed a second element, component, region, layer, or section withoutdeparting from the teachings of example embodiments.

Spatially relative terms (e.g., “beneath,” “below,” “lower,” “above,”“upper,” and the like) may be used herein for ease of description todescribe one element or feature's relationship to another element(s) orfeature(s) as illustrated in the figures. It should be understood thatthe spatially relative terms are intended to encompass differentorientations of the device in use or operation in addition to theorientation depicted in the figures. For example, if the device in thefigures is turned over, elements described as “below” or “beneath” otherelements or features would then be oriented “above” the other elementsor features. Thus, the term “below” may encompass both an orientation ofabove and below. The device may be otherwise oriented (rotated 90degrees or at other orientations) and the spatially relative descriptorsused herein interpreted accordingly.

The terminology used herein is for the purpose of describing variousembodiments only and is not intended to be limiting of exampleembodiments. As used herein, the singular forms “a,” “an,” and “the” areintended to include the plural forms as well, unless the context clearlyindicates otherwise. It will be further understood that the terms“includes,” “including,” “comprises,” and/or “comprising,” when used inthis specification, specify the presence of stated features, integers,steps, operations, elements, and/or components, but do not preclude thepresence or addition of one or more other features, integers, steps,operations, elements, components, and/or groups thereof.

Example embodiments are described herein with reference tocross-sectional illustrations that are schematic illustrations ofidealized embodiments (and intermediate structures) of exampleembodiments. As such, variations from the shapes of the illustrations asa result, for example, of manufacturing techniques and/or tolerances,are to be expected. Thus, example embodiments should not be construed aslimited to the shapes of regions illustrated herein but are to includedeviations in shapes that result, for example, from manufacturing.

Unless otherwise defined, all terms (including technical and scientificterms) used herein have the same meaning as commonly understood by oneof ordinary skill in the art to which example embodiments belong. Itwill be further understood that terms, including those defined incommonly used dictionaries, should be interpreted as having a meaningthat is consistent with their meaning in the context of the relevant artand will not be interpreted in an idealized or overly formal senseunless expressly so defined herein.

As used herein, the term “combination thereof” refers to a mutualsubstituent, a mixture, a stacked structure, etc.

As used herein, when a definition is not otherwise provided, the prefix“hetero” may refer to a group that includes 1 to 4 heteroatoms, eachindependently one of N, O, S, Si, and P. The total number of ringmembers may be 3 to 10. If multiple rings are present, each ring isindependently aromatic, saturated, or partially unsaturated, andmultiple rings, if present, may be fused, pendant, spirocyclic, or acombination thereof. Heterocycloalkyl groups include at least onenon-aromatic ring that contains a heteroatom ring member. Heteroarylgroups include at least one aromatic ring that contains a heteroatomring member. Non-aromatic and/or carbocyclic rings may also be presentin a heteroaryl group, provided that at least one ring is both aromaticand contains a ring member that is a heteroatom.

As used herein, when a definition is not otherwise provided, the term“alkyl group” may be a linear or branched saturated monovalenthydrocarbon group (e.g., a methyl group, an ethyl group, a propyl group,an isobutyl group, a sec-butyl group, a tert-butyl group, a pentylgroup, an iso-amyl group, a hexyl group, etc).

The term “aryl group” may refer to a monovalent functional group formedby the removal of one hydrogen atom from a ring of an arene, e.g.,phenyl or naphthyl. The arene may refer to a hydrocarbon having anaromatic ring, and includes monocyclic and polycyclic hydrocarbons,wherein the additional ring(s) of the polycyclic hydrocarbon may bearomatic or nonaromatic.

The “arylalkyl group” may refer to aryl group where at least onehydrogen atom is substituted with a lower alkylene, e.g., methylene,ethylene, propylene, etc. For example, the “arylalkyl group” may be abenzyl group or a phenylethyl group.

The term “cycloalkyl group” may refer to a monovalent functional grouphaving one or more saturated rings in which all ring members are carbon,e.g., a cyclopentyl group and a cyclohexyl group.

The term “heteroarylalkyl group” may refer to the alkyl group definedabove where at least one hydrogen atom is substituted with a heteroarylgroup.

The term “alkylheteroaryl group” may refer to the heteroaryl groupdefined above, where at least one hydrogen atom is substituted withalkyl group.

As used herein, when a definition is not otherwise provided, the term“aromatic ring” refers to a functional group in which all atoms in thecyclic functional group have a p-orbital, and wherein these p-orbitalsare conjugated. For example, the aromatic ring may be a C₆ to C₂₀ arylgroup.

As used herein, when a definition is not otherwise provided, the term“substituted” means that a compound or group is substituted with atleast one substituent independently selected from a halogen (—F, —Cl,—Br, or —I), a C₁ to C₃₀ linear or branched alkyl group, for example aC₁ to C₁₀ linear or branched alkyl group, a C₂ to C₃₀ linear or branchedalkenyl group, for example a C₂ to C₁₀ linear or branched alkenyl group,a C₂ to C₃₀ linear or branched alkynyl group, for example a C₂ to C₁₀linear or branched alkynyl group, a C₆ to C₃₀ aryl group, for example aC₆ to C₁₂ aryl group, a C₂ to C₃₀ heteroaryl group, for example a C₂ toC₁₂ heteroaryl group, a C₃ to C₃₀ cycloalkyl group, a C₁ to C₂₀fluoroalkyl group, a C₁ to C₂₀ perfluoroalkyl group (C_(n)F_(2n+1)), aC₁ to C₃₀ linear or branched alkoxy group, a C₃ to C₃₀ cycloalkoxygroup, a C₂ to C₃₀ linear or branched alkoxyalkyl group, a C₄ to C₃₀cycloalkoxyalkyl group, a cyano group, an amino group (—NRR′, whereineach of R and R′ is independently one of hydrogen or a C₁ to C₁₀ alkylgroup), an amidino group (—C(═NH)NH₂), a nitro group (—NO₂), an amidegroup (—C(═O)NHR, wherein R is hydrogen or a C₁ to C₁₀ alkyl group), analdehyde group (—C(═O)H), a hydroxy group (—OH), a sulfonyl group(—S(═O)₂R, wherein R is independently hydrogen or a C₁ to C₁₀ alkylgroup), and a carbamate group (—NHC(═O)OR, wherein R is a C₁ to C₁₀alkyl group), instead of hydrogen of the functional group or thecompound, provided that the substituted atom's normal valence is notexceeded.

According to example embodiments, a fused polycyclic heteroaromaticcompound is represented by Chemical Formula 1 and has a compact planarstructure in which a 5-membered or 6-membered aromatic ring are fusedtogether.

In Chemical Formula 1,

each of X¹ and X² is independently one of S, Se, and Te,

each of Y¹ to Y⁸ is independently one of nitrogen (N) and C—R^(a),wherein R^(a) is one of hydrogen and a linear or branched C₁ to C₁₀alkyl group, provided that at least one of Y¹ to Y⁴ and at least one ofY⁵ to Y⁸ are nitrogen, and

each of R¹ to R⁴ is independently one of hydrogen, a substituted orunsubstituted C₁ to C₃₀ alkyl group, a substituted or unsubstituted C6to C₃₀ aryl group and a substituted or unsubstituted C₂ to C₃₀heteroaryl group, a substituted or unsubstituted C₇ to C₃₀ arylalkylgroup, a substituted or unsubstituted C₂ to C₃₀ heteroarylalkyl group, asubstituted or unsubstituted C₂ to C₃₀ alkylheteroaryl group, asubstituted or unsubstituted C₅ to C₃₀ cycloalkyl group, and asubstituted or unsubstituted C₂ to C₃₀ heterocycloalkyl group.

In Chemical Formula 1, at least one of Y¹ to Y⁴ may be nitrogen (firstnitrogen) and at least one of Y⁵ to Y⁸ may be nitrogen (secondnitrogen), and the first nitrogen and the second nitrogen may bepositioned facing each other.

In Chemical Formula 1, at least two of Y¹ to Y⁴ may be nitrogen and atleast two of Y⁵ to Y⁸ may be nitrogen. For example, an aromatic ringpresent at the outmost may be a pyrimidine ring or a pyrazine ring.

The fused polycyclic heteroaromatic compound represented by ChemicalFormula 1 has a structure that six rings including aromatic rings andhetero aromatic rings are fused, of which the outmost aromatic ringcontains nitrogen. The nitrogen-containing aromatic ring may increase amolecular arrangement through a hydrogen bond among molecules, have anadvantage of packing and stacking the molecules, and resultantly showrelatively high charge mobility. When the molecular arrangement isincreased as above, a given or predetermined molecular arrangement ofthe compound may be induced during formation of a thin film through adeposition process, and thus thin film uniformity may be improved.

In addition, the fused polycyclic heteroaromatic compound is easilysynthesized to be effectively applied to a semiconductor material, anelectron transporting material, etc. By having a compact planarmolecular structure in which six aromatic rings and hetero aromaticrings are fused, oxidation potentials are relatively uniform and stablewhen the fused polycyclic heteroaromatic compound is applied to anactual device.

The fused polycyclic heteroaromatic compound represented by ChemicalFormula 1 may have a hydrogen bond by including a hetero atom selectedfrom S, Se, and Te present in a core aromatic ring and at least one N inthe outmost aromatic ring and thus improve a molecular interaction andprovide an advantageous packing structure for a charge transfer. Inaddition, the fused polycyclic heteroaromatic compound may have improvedthermal stability and thus improve heat resistance of a device.

The fused polycyclic heteroaromatic compound represented by ChemicalFormula 1 may include, for example, at least one of compounds (1) to (8)represented by Chemical Formula 1-1.

In Chemical Formula 1-1,

hydrogen of each aromatic ring may be replaced by a substituent, forexample a substituted or unsubstituted C₁ to C₃₀ linear or branchedalkyl group, a substituted or unsubstituted C6 to C₃₀ aryl group and asubstituted or unsubstituted C₂ to C₃₀ heteroaryl group, a substitutedor unsubstituted C₇ to C₃₀ arylalkyl group, a substituted orunsubstituted C₂ to C₃₀ heteroarylalkyl group, a substituted orunsubstituted C₂ to C₃₀ alkylheteroaryl group, a substituted orunsubstituted C₅ to C₃₀ cycloalkyl group, and a substituted orunsubstituted C₂ to C₃₀ heterocycloalkyl group.

According to example embodiments, a fused polycyclic heteroaromaticcompound is represented by one of Chemical Formula 2A and 2B.

In Chemical Formulae 2A and 2B,

each of X³ and X⁴ is independently one of S, Se, and Te,

each of R^(1a) and R^(1b) is independently one of hydrogen and a linearor branched C₁ to C₁₀ alkyl group, and

each of R¹² to R¹⁹ is independently one of hydrogen, a substituted orunsubstituted C₁ to C₃₀ alkyl group, a substituted or unsubstituted C6to C₃₀ aryl group and a substituted or unsubstituted C₂ to C₃₀heteroaryl group, a substituted or unsubstituted C₇ to C₃₀ arylalkylgroup, a substituted or unsubstituted C₂ to C₃₀ heteroarylalkyl group, asubstituted or unsubstituted C₂ to C₃₀ alkylheteroaryl group, asubstituted or unsubstituted C₅ to C₃₀ cycloalkyl group, and asubstituted or unsubstituted C₂ to C₃₀ heterocycloalkyl group.

The fused polycyclic heteroaromatic compound represented by ChemicalFormula 2A or 2B has a structure that six rings of aromatic rings andhetero aromatic ring are fused, of which the core aromatic ring containsnitrogen. The nitrogen-containing aromatic ring may increase a moleculararrangement through a hydrogen bond among molecules and thus have anadvantage of packing and stacking the molecules and resultantly, showhigh charge mobility. When the molecular arrangement is increased asabove, a constant molecular arrangement of the compound may be inducedduring formation of a thin film through a deposition process, and thinfilm uniformity may be improved.

In addition, the fused polycyclic heteroaromatic compound is easilysynthesized to be effectively applied to a semiconductor material, anelectron transporting material, etc. By having a compact planarmolecular structure in which six aromatic rings and hetero aromaticrings are fused, oxidation potentials are relatively uniform and stablewhen the fused polycyclic heteroaromatic compound is applied to anactual device.

The fused polycyclic heteroaromatic compound represented by ChemicalFormula 2A or 2B may have a hydrogen bond by including N in the corearomatic ring and a hetero atom selected from S, Se, and Te in theoutmost aromatic ring and thus improve a molecular interaction andprovide an advantageous packing structure for a charge transfer. Inaddition, the fused polycyclic heteroaromatic compound has improvedthermal stability and may improve heat resistance of a device.

The fused polycyclic heteroaromatic compound represented by ChemicalFormula 2A or 2B may include at least one of compounds (9) to (12)represented by Chemical Formula 2-1.

In Chemical Formula 2-1,

a hydrogen of each aromatic ring may be replaced by a substituent, forexample a substituted or unsubstituted C₁ to C₃₀ linear or branchedalkyl group, a substituted or unsubstituted C6 to C₃₀ aryl group and asubstituted or unsubstituted C₂ to C₃₀ heteroaryl group, a substitutedor unsubstituted C₇ to C₃₀ arylalkyl group, a substituted orunsubstituted C₂ to C₃₀ heteroarylalkyl group, a substituted orunsubstituted C₂ to C₃₀ alkylheteroaryl group, a substituted orunsubstituted C₅ to C₃₀ cycloalkyl group, and a substituted orunsubstituted C₂ to C₃₀ heterocycloalkyl group.

The HOMO energy, reorganization energy, and expectation mobility ofcompounds of compound (1) and compound (2) of the fused polycyclicheteroaromatic compound are calculated, and the results are shown inTable 1. The HOMO energy and the reorganization energy are calculated byusing a Gaussian 09 program in DFT B3LYP/6-31G (d, p) level, and atransfer integral is calculated by using the ADF (Amsterdam DensityFunctional) program at PW91-TZP, to calculate expectation mobilityaccording to Marcus theory. For comparison, the HOMO energy,reorganization energy, and expectation mobility of compounds of ref-1and ref-2 are also shown in Table 1.

TABLE 1 E_(HOMO) Reorganization Expectation mobility Compounds (eV)energy (meV) (rel.) (cm²/Vs) compound ref-1 −5.57 146 0.9 compound ref-2−5.59 218 0.14 compound (1) −5.77 149 1.5 compound (2) −5.90 153 1.6

As shown in Table 1, the compounds (1) and (2) have smallerreorganization energy compared with the compounds ref-1 and ref-2, andthus charges may be effectively transported among molecules. Thecompounds (1) and (2) exhibit higher expectation mobility compared withthe compounds ref-1 and ref-2.

The fused polycyclic heteroaromatic compound according to exampleembodiments may have a molecular weight of about 300 to about 3000, forexample 300 to 1000. Within the range of the average molecular weight,the fused polycyclic heteroaromatic compound may be relatively easy tohandle.

The fused polycyclic heteroaromatic compound may be prepared accordingto a general method, for example, chemical or electrochemical oxidationsynthesis, which is a representative method of polymerizing an aromaticcompound or a heteroaromatic compound, or condensation polymerizationusing a compound of an organic transition element, e.g., nickel orpalladium.

Example embodiments provide an organic thin film including the fusedpolycyclic heteroaromatic compound and an electronic device includingthe organic thin film.

The organic thin film according to example embodiments includes theaforementioned fused polycyclic heteroaromatic compound, and thus may beused as an organic semiconductor layer for an electronic device and acarrier transport layer, e.g., a channel layer, and the electronicdevice including the organic thin film shows improved electricalcharacteristics with high charge mobility as well as improvedprocessability and workability.

Herein, the organic thin film may be manufactured by depositing morethan one kind of the fused polycyclic heteroaromatic compound on asubstrate in a common method or dissolving the fused polycyclicheteroaromatic compound in an organic solvent and coating the solutionin a common room temperature solution process, and the deposited orcoated thin film may be heat-treated to increase density and uniformitythereof.

Particularly, the organic solvent may include at least one kind ofgeneral organic solvent, for example, at least one kind of an aliphatichydrocarbon solvent (e.g., hexane and/or heptane); an aromatichydrocarbon solvent (e.g., toluene, pyridine, quinoline, anisole,mesitylene and/or xylene); a ketone-based solvent (e.g., methyl isobutylketone, 1-methyl-2-pyrrolidinone, cyclohexanone and/or acetone); anether-based solvent (e.g., tetrahydrofuran and/or isopropyl ether); anacetate-based solvent (e.g., ethyl acetate, butyl acetate and/orpropylene glycol methyl ether acetate); an alcohol-based solvent (e.g.,isopropyl alcohol and/or butanol); an amide-based solvent (e.g.,dimethyl acetamide and/or dimethyl formamide); a silicone-based solvent;and a mixture of solvents. The amount of the fused polycyclicheteroaromatic compound dissolved in the organic solvent may beappropriately selected and determined by a person of ordinary skill inthe art, for example, in a range of about 0.01 wt % to about 50 wt %based on the total solution in view of solubility and coating property.

The method of providing an organic thin film may include thermaldeposition, vacuum deposition, laser deposition, screen printing,printing, imprinting, spin casting, dipping, ink jetting, roll coating,flow coating, drop casting, spray coating, and/or roll printing, but isnot limited thereto. The heat treatment may be performed at about 80 toabout 250° C. for about 1 minute to about 2 hours, but is not limitedthereto.

The thickness of the organic thin film may be adjusted according to theusage and the case considering the kinds of the used compound andsolvent by a person of ordinary skill in the art, and is specifically ina range of about 200 Å to about 10,000 Å.

Examples of electronic devices including the organic thin film as acarrier transport layer may include a transistor, an organic lightemitting diode (OLED), a photovoltaic device, a solar cell, a laserdevice, a memory, and/or a sensor, and the organic thin film may beapplied to each device according to the general process commonly knownin the art.

For example, the transistor includes a gate electrode disposed on asubstrate, a source electrode and a drain electrode facing each otherand defining a channel region, an insulation layer electricallyinsulating the source electrode and drain electrode and the gateelectrode, and an active layer including the fused polycyclicheteroaromatic compound formed in the channel region.

The active layer may be obtained by depositing the fused polycyclicheteroaromatic compound, or applying a composition including the fusedpolycyclic heteroaromatic compound to a solution process, for example,screen printing, printing, spin coating, dipping, and/or ink jetting.When the active layer is formed by the solution process, the processcost may be reduced, and a large area device may be effectivelymanufactured.

FIGS. 1 and 2 are schematic cross-sectional views showing a transistoraccording to example embodiments. The transistor according to exampleembodiments may be a thin film transistor. The thin film transistor maybe a thin film having a thickness of several nanometers to severalmicrons.

Referring to FIG. 1, a transistor 10 includes a substrate 12, a gateelectrode 14 disposed on the substrate, and an insulation layer 16covering the gate electrode 14. A source electrode 17 a and a drainelectrode 17 b defining a channel region are provided on the insulationlayer 16, and an active layer 18 is provided in the channel region. Theactive layer 18 includes the fused polycyclic heteroaromatic compound.

Referring to FIG. 2, a transistor 20 includes a source electrode 27 aand a drain electrode 27 b defining a channel region and that are formedon a substrate 22, and an active layer 28 formed on the channel region.The active layer 28 includes the fused polycyclic heteroaromaticcompound. An insulation layer 26 is formed to cover the source electrode27 a, the drain electrode 27 b, and the active layer 28, and a gateelectrode 24 is formed thereon.

The substrates 12 and 22 may include an inorganic material, an organicmaterial, or a composite of an inorganic material and an organicmaterial. The organic material may include, for example, a plastic(e.g., polyethylene naphthalate (PEN), polyethylene terephthalate (PET),polycarbonate, polyvinyl alcohol, polyacrylate, polyimide,polynorbornene, and polyethersulfone (PES)), and the inorganic materialmay include, for example, glass or metal.

In addition, the gate electrodes 14 and 24, source electrodes 17 a and27 a, and drain electrodes 17 b and 27 b may include a generally-usedmetal, particularly, gold (Au), silver (Ag), aluminum (Al), nickel (Ni),or indium tin oxide (ITO), but is not limited thereto.

The insulation layers 16 and 26 may include a generally-used insulatorhaving a high dielectric constant, for example, a ferroelectricinsulator (e.g., Ba_(0.33)Sr_(0.66)TiO₃ (BST, barium strontiumtitanate), Al₂O₃, Ta₂O₅, La₂O₅, Y₂O₃ and/or TiO₂); an inorganicinsulator (e.g., PbZr_(0.33)Ti_(0.66)O₃ (PZT), Bi₄Ti₃O₁₂, BaMgF₄,SrBi₂(TaNb)₂O₉, Ba(ZrTi)O₃ (BZT), BaTiO₃, SrTiO₃, SiO₂, SiN_(x) (x isdetermined depending on valence of Si), and/or AlON (aluminumoxynitride)); or an organic insulator (e.g., polyimide, benzocyclobutane(BCB), parylene, polyacrylate, polyvinyl alcohol, and polyvinylphenol),but is not limited thereto.

Hereinafter, the embodiments are illustrated in more detail withreference to examples. However, these are examples, and the presentdisclosure is not limited thereto.

EXAMPLE 1 Synthesis of Compound (1)

(1) Synthesis ofThieno[3,2,b]thiophene-2,5-diylbis((2-bromopyridin-3-yl)methanol(Compound 1a)

Thienothiophene dicarbaldehyde (5 g, 25.48 mmol) is dissolved in 250 mLof dry diethylether and dry tetrahydrofuran and then, cooled down to−78° C. 42.12 mL of lithium diisopropylamine (a 2.0 M hexane solution)is slowly added thereto in a dropwise fashion, and 2,3-dibromopyridine(13.3 g, 56.16 mmol) is added thereto. The temperature is slowlyincreased, and the mixture is stirred at room temperature (24° C.) for12 hours. Then, 100 mL of an ammonium chloride-saturated solution isadded thereto, and an extract is obtained by using chloroform andseveral times washed with water. The extract is dried with magnesiumsulfate and filtered, and the chloroform solvent is removed to obtain acompound 1a. (a yield of 75%)

(2) Synthesis of2,5-bis(2-bromopyridin-3-yl)methyl)thieno[3,2,b]thiophene (Compound 1b)

The compound 1a (9.8 g, 19.13 mmol) is dissolved in 300 mL ofdichloromethane, and ZnI₂ (19.54 g, 61.22 mmol) and NaCNBH₃ (16.83 g,267.8 mmol) are slowly added thereto. The mixture is stirred at roomtemperature (24° C.) for 24 hours and passed through a Celite pad. Thefiltered solution is respectively washed with an ammonium chloridesaturated solution and water, dried with MgSO₄, and concentrated under areduced pressure to obtain yellow oil. This obtained material ispurified through silica chromatography, obtaining a desired compound 1b.(a yield of 80%)

(3) Synthesis of3,3′-(thieno[3,2,b]thiophen-2,5-diylbis(methylene))dipicolinealdehyde(Compound 1c)

A tetrahydrofuran solution (100 mL) in which the compound 1b (5.7 g,11.13 mmol) is dissolved is added in a dropwise fashion to the diethylether (200 mL) solution in which t-butyl lithium (30.11 mmol) isdissolved and cooled down to −78° C. The mixed solution is stirred at−78° C. for about 30 minutes, dimethylformaldehyde (2.44 g) is addedthereto, and the obtained mixture is stirred for about 2 hours again.When the reaction is completed by pouring water thereinto, 200 mL ofethyl acetate is added thereto, the mixture is washed with water andbrine, and an organic layer produced therein is dried with MgSO₄ andconcentrated under a reduced pressure, obtaining colorless oil. Thisobtained material is purified through silica chromatography, obtaining adesired compound 1c (a yield of 50%).

(4) Synthesis of Compound (1)

30 mL of the compound 1c (2.1 g) is dissolved in benzene, Amberlyst 15(0.5 g) is added thereto, and water is removed therefrom by using aDean-Stark trap while the mixture is stirred and refluxed. After 24hours, a yellow solid is precipitated. The temperature is cooled down toroom temperature (24° C.), the Amberlyst 15 is precipitated and then,filtered after taking off a floater therefrom, obtained a desiredcompound 1 as a yellow solid (a yield of 60%).

The MALDI-MS analysis result of the compound 1 is provided in FIG. 3.

Maldi-MS m/z=342.76 (M+1).

EXAMPLE 2 Synthesis of Compound (2)

(1) Synthesis ofThieno[3,2,b]thiophene-2,5-diylbis((3-bromopyridin-3-yl)methanol(Compound 2a)

Thienothiophene dicarbaldehyde (5 g, 25.48 mmol) is dissolved in 250 mLof dry diethylether and dry tetrahydrofuran (THF) and then, cooled downto −78° C. Then, 42.12 mL of diisopropylamine (a 2.0 M hexane solution)is slowly added thereto in a dropwise fashion, and 2,3-dibromopyridine(13.3 g, 56.16 mmol) is added thereto. The mixture is slowly heated andstirred at room temperature (24° C.) for 12 hours. Subsequently, 100 mLof an ammonium chloride-saturated solution is added thereto, and anextract is obtained by using chloroform and several times washed withwater. The obtained extract is dried with magnesium sulfate and then,filtered, and the chloroform solvent is removed to obtain a compound 2a.(a yield of 75%)

(2) Synthesis of2,5-bis(3-bromopyridin-3-yl)methyl)thieno[3,2,b]thiophene (Compound 2b)

The compound 2a (9.8 g, 19.13 mmol) is dissolved in 300 mL ofdichloromethane, and ZnI₂ (19.54 g, 61.22 mmol) and NaCNBH₃ (16.83 g,267.8 mmol) are slowly added thereto. The mixture is stirred at roomtemperature (24° C.) for 24 hours and passed through a Celite pad. Thefiltered solution is respectively washed with an ammoniumchloride-saturated solution and water, dried with MgSO₄, andconcentrated under a reduced pressure, obtaining yellow oil. Thisobtained material is purified through silica chromatography, obtaining adesired compound 2b. (a yield of 80%)

(3) Synthesis of4,4′-(thieno[3,2-b]thiophene-2,5-diylbis(methylene))dinicotinaldehyde(Compound 2c)

A tetrahydrofuran solution (100 mL) in which the compound 2b (5.7 g,11.13 mmol) is dissolved is slowly added in a dropwise fashion to adiethyl ether (200 mL) solution in which t-butyl lithium (30.11 mmol) isdissolved and cooled down to −78° C. The mixture is stirred at −78° C.for about 30 minutes, dimethylformaldehyde (2.44 g) is added thereto,and the obtained mixture is stirred again for about 2 hours. When thereaction is completed by pouring water thereinto, 200 mL of ethylacetate is added thereto, the mixture is washed with water and brine,and an organic layer produced therein is dried with MgSO₄, andconcentrated under a reduced pressure, obtaining colorless oil. Thisobtained material is purified through silica chromatography, obtaining adesired compound 2c (a yield of 50%).

(4) Synthesis of Compound (2)

The compound 2c (2.1 g) is dissolved in 30 mL of benzene, Amberlyst 15(0.5 g) is added thereto, and water is removed therefrom by using aDean-Stark trap while the mixture is stirred and refluxed. After 24hours or so, a yellow solid is precipitated. The temperature is cooleddown to room temperature (24° C.), the Amberlyst 15 is precipitated andthen, filtered after taking off a floater therefrom, obtaining a desiredcompound 2 as a yellow solid (a yield of 60%).

The thermogravimetric analysis result (TGA) of the compound 1 isprovided in FIG. 4. As shown in FIG. 4, a temperature when 5 wt % of thecompound 1 is decreased is 383.02° C. Accordingly, the compound 1 turnsout to have improved thermal stability.

EXAMPLE 3 Manufacture of Organic Thin Film Transistor (OTFT)

First, chromium used as a gate electrode is deposited to be 1000 Å thickthrough sputtering on a cleaned glass substrate, and SiO₂ is depositedto form a 3000 Å-thick insulation layer thereon in a CVD method. Then,Au is deposited thereon to be 700 Å thick through sputtering, forming asource electrode and a drain electrode. The glass substrate is cleanedwith isopropyl alcohol for 10 minutes and dried before coating anorganic semiconductor material. In addition, the SiO₂ used as aninsulation layer is treated with UV/O₃ for 30 minutes before surfacemodification.

Then, an OTFT device 10 having a structure shown in FIG. 1 ismanufactured by dipping the substrate in n-hexane and anoctyltrichlorosilane solution diluted into a concentration of 10 mM for30 minutes, washing the substrate with hexane and alcohol, drying thesubstrate, and thermally evaporating the compound (1) synthesizedaccording to Example 1 under high vacuum (5×10⁻⁶ torr) at a speed of 0.2Å/sec to form a 1000 Å-thick active layer 18.

EXAMPLE 4 Manufacture of Organic Thin Film Transistor (OTFT)

An OTFT device is manufactured according to the same method as inExample 3, except that the compound 2 is used instead of the compound 1.

While this disclosure has been described in connection with what ispresently considered to be practical example embodiments, it is to beunderstood that the present inventive concepts are not limited to thedisclosed embodiments, but, on the contrary, is intended to covervarious modifications and equivalent arrangements included within thespirit and scope of the appended claims.

What is claimed is:
 1. An electronic device comprising: a fusedpolycyclic heteroaromatic compound represented by one of ChemicalFormula 2A and Chemical Formula 2B,

wherein, in Chemical Formulae 2A and 2B, each of X³ and X⁴ isindependently one of S, Se, and Te, each of R^(1a) and R^(1b) isindependently one of hydrogen and a linear or branched C₁ to C₁₀ alkylgroup, and each of R¹² to R¹⁹ is independently one of hydrogen, asubstituted or unsubstituted C₁ to C₃₀ alkyl group, a substituted orunsubstituted C₆ to C₃₀ aryl group and a substituted or unsubstituted C₂to C₃₀ heteroaryl group, a substituted or unsubstituted C₇ to C₃₀arylalkyl group, a substituted or unsubstituted C₂ to C₃₀heteroarylalkyl group, a substituted or unsubstituted C₂ to C₃₀alkylheteroaryl group, a substituted or unsubstituted C₅ to C₃₀cycloalkyl group, and a substituted or unsubstituted C₂ to C₃₀heterocycloalkyl group, wherein the electronic device is a transistor, aphotovoltaic device, a solar cell, a laser device, a memory device, or asensor.
 2. The electronic device of claim 1, wherein the fusedpolycyclic heteroaromatic compound has a molecular weight of about 300to about 3,000.
 3. The electronic device of claim 1, wherein the fusedpolycyclic heteroaromatic compound represented by Chemical Formula 2A or2B comprises at least one of compounds (9) to (12) represented byChemical Formula 2-1:

wherein, in Chemical Formula 2-1, a hydrogen of each aromatic ring isreplaced by a substituted or unsubstituted C₁ to C₃₀ linear or branchedalkyl group, a substituted or unsubstituted C₆ to C₃₀ aryl group and asubstituted or unsubstituted C₂ to C₃₀ heteroaryl group, a substitutedor unsubstituted C₇ to C₃₀ arylalkyl group, a substituted orunsubstituted C₂ to C₃₀ heteroarylalkyl group, a substituted orunsubstituted C₂ to C₃₀ alkylheteroaryl group, a substituted orunsubstituted C₅ to C₃₀ cycloalkyl group, and a substituted orunsubstituted C₂ to C₃₀ heterocycloalkyl group.
 4. The electronic deviceof claim 3, wherein the fused polycyclic heteroaromatic compound has amolecular weight of about 300 to about 3,000.
 5. The electronic deviceof claim 1, further comprising: an organic thin film comprising thefused polycyclic heteroaromatic compound.
 6. The electronic device ofclaim 3, wherein the fused polycyclic heteroaromatic compound isrepresented by compound
 10. 7. The electronic device of claim 3, whereinthe fused polycyclic heteroaromatic compound is represented by compound11.
 8. The electronic device of claim 3, wherein the fused polycyclicheteroaromatic compound is represented by compound
 12. 9. The electronicdevice of claim 1, wherein the electronic device is a transistor. 10.The electronic device of claim 1, wherein the electronic device is aphotovoltaic device.
 11. The electronic device of claim 1, wherein theelectronic is a solar cell.
 12. The electronic device of claim 1,wherein the electronic device is a laser device.
 13. The electronicdevice of claim 1, wherein the electronic device is a memory device. 14.The electronic device of claim 1, wherein the electronic device is asensor.